Canonical Allele Identifier: CA360063026
Gene: HEXB HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.73985231A>C (hg19) chr5:g.74689406A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.74689406A>C , CM000667.2:g.74689406A>C GRCh38
NC_000005.9:g.73985231A>C , CM000667.1:g.73985231A>C GRCh37
NC_000005.8:g.74020987A>C NCBI36
NG_009770.1:g.9263A>C
NG_009770.2:g.54384A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261416.12:c.378A>C MANE Select ENSP00000261416.7:p.Gln126His
ENST00000261416.11:c.378A>C ENSP00000261416.7:p.Gln126His
ENST00000511181.5:c.-298A>C ENSP00000426285.1:n.-298A>C
ENST00000513079.5:n.443A>C
ENST00000515528.1:n.433A>C
NM_000521.3:c.378A>C NP_000512.1:p.Gln126His
NM_001292004.1:c.-298A>C NP_001278933.1:n.-298A>C
NM_000521.4:c.378A>C MANE Select NP_000512.2:p.Gln126His
NM_001292004.2:c.-298A>C NP_001278933.1:n.-298A>C
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